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Genetic Overlap between Holoprosencephaly and Kallmann Syndrome
Patients with Kallmann syndrome (KS; congenital hypogonadotropic hypogonadism and decreased/absent sense of smell), septo-optic dysplasia (SOD), or holoprosencephaly (HPE) reportedly have midline defects. In this study, we investigate a genetic overlap between KS, SOD, and HPE. Nineteen subjects (18...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
S. Karger AG
2012
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3398826/ https://ncbi.nlm.nih.gov/pubmed/22855648 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000338706 |
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